50707-41-0 Usage
General Description
1-ISOPROPYL-3-P-TOLYLTRIAZENE, also known as IPT, is a chemical compound with the molecular formula C10H14N4. It is a clear to light yellow liquid with a slightly aromatic odor. IPT is commonly used as a radical inhibitor and stabilizer in various industrial processes, such as the production of rubber and plastics, as well as in the manufacture of paint and coatings. It functions by scavenging free radicals and preventing chain reactions that can lead to degradation and instability of the final product. Additionally, IPT has been studied for its potential use as a novel therapy for cancer, due to its ability to inhibit tumor cell growth and induce apoptosis. However, further research is necessary to fully understand its potential medicinal applications.
Check Digit Verification of cas no
The CAS Registry Mumber 50707-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50707-41:
(7*5)+(6*0)+(5*7)+(4*0)+(3*7)+(2*4)+(1*1)=100
100 % 10 = 0
So 50707-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N3/c1-8(2)11-13-12-10-6-4-9(3)5-7-10/h4-8H,1-3H3,(H,11,12)
50707-41-0Relevant articles and documents
STRUCTURAL EFFECT ON THE MECHANISTIC PATHWAY OF THE DECOMPOSITION OF 3-ALKYL-1-ARYLTRIAZENES: A KINETIC STUDY
Laila, Abdulhameed A. R.
, p. 453 - 456 (2007/10/02)
A kinetic study of the reaction between 3-alkyl-1-aryltriazenes and substituted acetic acids has been made in solvent acetone over the temperature range 21-37 deg C.Ea is 17.3 +/- 0.3 kcal mol-1 and log A is 10.3 +/- 0.1.Influence of the substituents on the reaction rate has been analyzed.The Hammett correlation with ? gave a ρ value of -0.96 for para-aryl substituted triazenes and +0.35 for meta- and para-substituted phenylacetic acid.The rate of decomposition of triazenes is also affected by changing the alkyl group.From these results a duality in mechanism is proposed; first, a simultaneous protonation and alkyl group expulsion to be the rate-determining step when R is tertiary, benzylic and possibly secondary.Secondly, a concerted mechanism for the protonation of nitrogen and cleavage of the N-R bond for primary alkyl groups.
